STUDIO 35
- Product NDC
- 0363-7215
- 11-digit product format
- 003637215
- Labeler code
- 0363
- Product ID
- 0363-7215_1e0b6871-f060-43ba-aa12-0313c31a39e1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- WALGREEN COMPANY
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-07-08
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0363-7215-60 | STUDIO 35AMBER | 1650 mL in 1 BOTTLE, PLASTIC | LIQUID | 1650 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-7215 | STUDIO 35 AMBER (BENZALKONIUM CHLORIDE) LIQUID [WALGREEN COMPANY] | 1 | Legacy NDC, 1 package rows | 20130709_17246846-3e26-4591-882f-69fe556a7a05.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 0363-7215-60 | 00363721560 | 1650 mL in 1 BOTTLE, PLASTIC | 1650 ml | Historical |